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Gene HMID Gene Symbol Organ Specificity DiseaseID Disease Name Related Organ
HM01459FBXO15blood vesselMESH:D011565Psoriasisskin
HM01459FBXO15blood vesselMESH:D003924Diabetes Mellitus, Type 2pancreas
HM01459FBXO15blood vesselMESH:D007638Keratoconjunctivitis Siccaeye
HM01459FBXO15blood vesselMESH:D003920Diabetes Mellituspancreas
HM01459FBXO15blood vesselMESH:D005234Fatty Liver
HM01459FBXO15blood vesselMESH:D014985Xerophthalmiaeye
HM01459FBXO15blood vesselMESH:D004487Edema
HM01459FBXO15blood vesselMESH:D007249Inflammation
HM01459FBXO15blood vesselMESH:D007333Insulin Resistance
HM01459FBXO15blood vesselMESH:D000544Alzheimer Diseasenerve
HM01459FBXO15blood vesselMESH:D005355Fibrosis
HM01459FBXO15blood vesselMESH:D008106Liver Cirrhosis, Experimental
HM01459FBXO15blood vesselMESH:D009402Nephrosis, Lipoidkidney
HM01459FBXO15blood vesselMESH:D006457Hemoglobinuria, Paroxysmal
HM01459FBXO15blood vesselMESH:D009404Nephrotic Syndromekidney
HM01459FBXO15blood vesselMESH:D007674Kidney Diseasesureter
HM01459FBXO15blood vesselMESH:D007674Kidney Diseasespituitary
HM01459FBXO15blood vesselMESH:D007674Kidney Diseaseskidney
HM01459FBXO15blood vesselMESH:D008325Mammary Neoplasms, Experimental
HM01459FBXO15blood vesselMESH:D014605Uveitiseye
HM01459FBXO15blood vesselMESH:D024821Metabolic Syndrome X
HM01459FBXO15blood vesselMESH:D008664Metal Metabolism, Inborn Errorsskin
HM01459FBXO15blood vesselMESH:D008664Metal Metabolism, Inborn Errorsmuscle
HM01459FBXO15blood vesselMESH:D008664Metal Metabolism, Inborn Errorsliver
HM01459FBXO15blood vesselMESH:D008664Metal Metabolism, Inborn Errorskidney
HM01459FBXO15blood vesselMESH:D006930Hyperalgesia
HM01459FBXO15blood vesselMESH:D006973Hypertensionlung
HM01459FBXO15blood vesselMESH:D006973Hypertensionheart
HM01459FBXO15blood vesselMESH:D006973Hypertensionblood vessel
HM01459FBXO15blood vesselMESH:D005885Gingival Hyperplasia